Medical Management of Castration Resistant Prostate
Cancer (CRPC): Beyond Chemotherapy
Volume 2 - Issue 5
Ganesh K Bakshi1, SK Raghunath2, Sudhir Rawal3, Ganesh Gopalakrishnan4, Sanjai K Addla5, Priya J6, Suyog C
Mehta7, Mrinal Borgohain7 and Rajan Mittal7*
-
Author Information
Open or Close
- 1Department of Urology, Tata Memorial Hospital, India
- 2Department of Urology, HCG Cancer Care, India
- 3Department of Urology, Rajiv Gandhi Cancer Institute and Research Centre, India
- 4Vedanayagam Hospital Pvt. Ltd., India
- 5Department of Urology, Apollo Hospital, India
- 6Department of Urology, Joshi Hospital, India
- 7Medical Affairs, Dr. Reddy’s Laboratories Ltd, India
*Corresponding author:
Dr. Rajan Mittal, MD, DM (Clinical Pharmacology) Director, Medical Affairs at Dr. Reddy’s Laboratories Ltd,
7-1-27, Ameerpet, Hyderabad, India
Received: March 03, 2020, 2020; Published: March 12, 2020
DOI: 10.32474/JUNS.2020.02.000146
Full Text
PDF
To view the Full Article Peer-reviewed Article PDF
Abstract
Prostate cancer is one of the leading causes of cancer-related mortality in men. Despite advances in treatment options, about
30-40% of patients develop the advanced disease in due course. Androgen deprivation is the standard first-line systemic therapy for
men with advanced prostate cancer. Almost all patients with the metastatic disease go on to develop castration-resistant prostate
cancer. The multiple therapeutic alternatives for castration-resistant prostate cancer, including abiraterone acetate, enzalutamide,
cabazitaxel, immunotherapy with sipuleucel-T, radiopharmaceuticals and bone-targeted therapies (zoledronic acid, denosumab)
along with docetaxel have made the decision-making process complex and challenging for clinicians. Even the strong pipeline of
systemic therapies with a diverse array of mechanisms of action in prostate cancer have shown preliminary signs of clinical benefit,
leading to more definitive phase III confirmatory trials. The review will relate the pathogenesis to the management of castrationresistant
prostate cancer and look for the best therapy approaches in metastatic castration-resistant prostate cancer, needed to
tackle the existing challenges effectively.
Keywords: Castration Resistant Prostate Cancer; Prostate Cancer; AR signaling inhibitor; metastatic; asymptomatic
Abbreviations: GLOBOCAN: Global Cancer Incidence, Mortality and Prevalence; CRPC: castration-resistant prostate cancer; mPC:
metastatic prostate cancer; mCRPC: metastatic castration-resistant prostate cancer; NM-CRPC: non-metastatic CRPC; FDA: Food
and Drug Administration; PSA: prostate-specific antigen; EAU: European Association of Urology; AA: abiraterone acetate; RECIST:
Response Evaluation Criteria in Solid Tumors; ADT: androgen deprivation therapy; LBD: ligand binding domain; MAPK : mitogenactivated
protein kinases; BRCA: breast cancer gene; ATM: ataxia telangiectasia mutated; AUA: American Urological Association;
NEPC: Neuroendocrine prostate cancer
Abstract|
Introduction|
Conclusion|
Acknowledgement|
Disclosure Statement|
References|